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Shinhung MST Co., Ltd.

US

Last updated May 24, 2026

What Shinhung MST Co., Ltd. makes

Shinhung MST Co., Ltd. manufactures dental implant suprastructures, including permanent and temporary preformed designs, as well as kits for dental implant procedures. Their portfolio also includes screw endosteal dental implants in both one-piece and two-piece configurations, reusable dental drill bits, and various surgical procedure kits for dental and maxillofacial applications. These products are designed for single-use and reusable medical settings, depending on the device type.

The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Their products are regulated under U.S. medical device laws, ensuring compliance with applicable standards for dental and surgical instruments. The manufacturer operates from the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Shinhung MST Co., Ltd. primarily manufacture?

Shinhung MST Co., Ltd. specializes in dental and maxillofacial medical devices. Their portfolio includes dental implant suprastructures (both permanent and temporary preformed types), screw endosteal dental implants (available in one-piece or two-piece designs), reusable dental drill bits, and various surgical procedure kits. These kits are designed for dental and maxillofacial procedures, with some intended for single-use and others for reusable applications.

Where is Shinhung MST Co., Ltd. based, and how does this affect their regulatory compliance?

Shinhung MST Co., Ltd. is based in the United States, which means their devices are subject to U.S. medical device regulations. Since they operate within the U.S., their products must comply with FDA requirements, including classification under FDA’s regulatory framework (Class I or Class II) and registration in the FDA’s Unique Device Identifier (UDI) database.

Which regulatory registries or databases list Shinhung MST Co., Ltd.’s devices?

Shinhung MST Co., Ltd.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S., ensuring transparency and traceability for healthcare providers and regulators.

How are Shinhung MST Co., Ltd.’s devices classified under U.S. regulations?

Shinhung MST Co., Ltd.’s devices fall under two FDA classification categories: Class I and Class II. Class I devices generally pose the lowest risk and may require general controls, while Class II devices involve a higher level of risk and require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and regulatory history.

What kinds of surgical kits does Shinhung MST Co., Ltd. produce, and how are they categorized?

Shinhung MST Co., Ltd. manufactures both dental implant procedure kits and general/maxillofacial surgical kits. These kits are categorized based on their intended use—some are designed for single-use (non-medicated), while others are reusable. For example, their dental/maxillofacial surgical kits are reusable, whereas general surgical procedure kits may be intended for single-use applications, depending on the specific product.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
+821099545139
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
689667152

Catalogue (1225)

Page 18 of 25
DeviceModel / ReferenceRegistriesClassStatus
St STW4511SSF
FDA UDI
Class IIActive
evertis NSSD3510
FDA UDI
Class IActive
evertis ZTBCS64
FDA UDI
Class IActive
Si SIR5011SF
FDA UDI
Class IIActive
Surgical Kit LCB35
FDA UDI
Class IActive
Si SMAR01
FDA UDI
Class IIActive
Si SSA45R30
FDA UDI
Class IIActive
S-Guide Kit TDR4010
FDA UDI
Class IActive
Si SIDAR6043H
FDA UDI
Class IIActive
evertis NSSD4508
FDA UDI
Class IActive
Si SIDAR6072
FDA UDI
Class IIActive
Si SSA45R20
FDA UDI
Class IIActive
Si NSIN3508SF
FDA UDI
Class IIActive
Si SIDAR6051H
FDA UDI
Class IIActive
Se EBCR5064H
FDA UDI
Class IActive
evertis NSSD3508
FDA UDI
Class IActive
Si SAT55H
FDA UDI
Class IActive
St EASR01
FDA UDI
Class IIActive
St STDAW70
FDA UDI
Class IIActive
Si SDAN5041H
FDA UDI
Class IIActive
Short Drill Kit SSD5006
FDA UDI
Class IActive
S-Guide Kit ADH10
FDA UDI
Class IActive
S-Guide Kit SSGR57C
FDA UDI
Class IActive
Si SIDAR5072H
FDA UDI
Class IIActive
Surgical Kit SBPR65
FDA UDI
Class IActive
Si SIDAN4554H
FDA UDI
Class IIActive
Si SAA4515R20HF
FDA UDI
Class IIActive
evertis MRTR
FDA UDI
Class IActive
Si SDAN4554
FDA UDI
Class IIActive
Surgical Kit SSD2007A
FDA UDI
Class IActive
evertis TBBCSR44
FDA UDI
Class IActive
Sm MB3011SR
FDA UDI
Class IIActive
St STR4010LS
FDA UDI
Class IIActive
Surgical Kit TWFA00NS
FDA UDI
Class IActive
Si SIR5008S
FDA UDI
Class IIActive
Si SIDAR6051
FDA UDI
Class IIActive
Si SFTN40L
FDA UDI
Class IActive
S-Guide Kit TDW5011
FDA UDI
Class IActive
Si SDAR6045H
FDA UDI
Class IIActive
Sm MBTCP
FDA UDI
Class IIActive
Surgical Kit STHFD01L
FDA UDI
Class IActive
Se EBCR5066H
FDA UDI
Class IActive
Si SHAN5050
FDA UDI
Class IIActive
Si SDAN4553H
FDA UDI
Class IIActive
evertis NSSD5011
FDA UDI
Class IActive
Surgical Kit SHS02S
FDA UDI
Class IActive
Si SFTR60L
FDA UDI
Class IActive
Si STAR5030H
FDA UDI
Class IIActive
evertis TBBCN5043R
FDA UDI
Class IActive
Sinus Kit SIDR37
FDA UDI
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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Notified Bodies

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Authorities

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Shinhung MST Co., Ltd. Wonju Si Gangwon · KR FEI 3006948193